A Dominant Mutation in the Gene Encoding the Erythroid Transcription Factor KLF1 Causes a Congenital Dyserythropoietic Anemia

Lionel Arnaud, Carole Saison, Virginie Helias, +20

The American Journal of Human Genetics

Transcriptional RegulationDevelopmental BiologyGenetic DisorderGeneticsInherited Metabolic Disease +8

Mutation of a Gene Essential for Ribosome Biogenesis, EMG1, Causes Bowen-Conradi Syndrome

Joy Armistead, Sunita Khatkar, Britta Meyer, +13

The American Journal of Human Genetics

Genome InstabilityRibosome BiogenesisMendelian DisorderGenetic DisorderGenetics +6

GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome

Dan Doherty, Albert E. Chudley, Gail Coghlan, +15

The American Journal of Human Genetics

Mendelian DisorderBrain MalformationsGenetic DisorderGeneticsPathology +5

A Gene for Autosomal Recessive Limb-Girdle Muscular Dystrophy in Manitoba Hutterites Maps to Chromosome Region 9q31-q33: Evidence for Another Limb-Girdle Muscular Dystrophy Locus

Tracey Weiler, Cheryl R. Greenberg, Teresa Zelinski, +6

The American Journal of Human Genetics

Genetic AnalysisDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics +5

Helicobacter Pylori in The Canadian Arctic: Seroprevalence and Detection in Community Water Samples

Iris McKeown, Pamela Orr, Sharon Macdonald, +8

The American Journal of Gastroenterology

ABCG2 null alleles define the Jr(a−) blood group phenotype

Teresa Zelinski, Gail Coghlan, Xiaoqing Liu, +1

Nature Genetics

Allelic VariantBlood Group PhenotypeMedicineGeneticsHematology +6

A novel mutation in <i>KIAA0196</i>: identification of a gene involved in Ritscher–Schinzel/3C syndrome in a First Nations cohort

Alison M. Elliott, Louise R. Simard, Gail Coghlan, +7

Journal of Medical Genetics

Seroprevalence of Helicobacter pylori, Incidence of Gastric Cancer, and Peptic Ulcer-Associated Hospitalizations in a Canadian Indian Population

Çharles N. Bernstein, Iris McKeown, John M. Embil, +9

Digestive Diseases and Sciences

Molecular definition of red cell Rh haplotypes by tightly linked SphI RFLPs.

Chi‐Hsiang Huang, M. E. Reid, Y Chen, +2

PubMed

Genetic linkage between the Kell blood group system and prolactin‐inducible protein loci: provisional assignment of KEL to chromosome 7

Teresa Zelinski, Gail Coghlan, Yvonne Myal, +4

Annals of Human Genetics